Study of a Topical Formulation for the Treatment and Prevention of Raynaud's Phenomenon Symptoms

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2010 by MediQuest Therapeutics.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
MediQuest Therapeutics
ClinicalTrials.gov Identifier:
NCT00934427
First received: June 26, 2009
Last updated: July 19, 2010
Last verified: July 2010
  Purpose

The purpose of this study is to determine if Vascana, a novel topical formulation of nitroglycerin, is effective in the treatment and prevention of the symptoms associated with Raynaud's Phenomenon.


Condition Intervention Phase
Raynaud Disease
Drug: 0.9% nitroglycerin in TAM cream
Drug: vehicle cream
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Study of a Topical Formulation of Nitroglycerin, Vascana® (MQX-503), and Matching Vehicle in the Treatment and Prevention of Symptoms Associated With Raynaud's Phenomenon

Resource links provided by NLM:


Further study details as provided by MediQuest Therapeutics:

Primary Outcome Measures:
  • Response rate as measured by changes in severity of the Raynaud's symptom most bothersome to the individual patient (Pain, Numbness, or Tingling) [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Changes from baseline in severity of each Raynaud's symptom (Pain, Numbness, and Tingling) [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Changes from baseline in duration of Raynaud's attacks [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Changes from baseline in number of Raynaud's attacks [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Changes from baseline in the Raynaud's Condition Score [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Changes in the maximum reduction in skin temperature [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Changes from baseline in overall disease severity measures [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
  • Changes in the time to return to baseline skin temperature [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 100
Study Start Date: June 2009
Estimated Study Completion Date: July 2010
Estimated Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Vascana Drug: 0.9% nitroglycerin in TAM cream
0.5 g of Vascana (0.9% nitroglycerin in proprietary vehicle cream) is applied topically BID for one day before certain planned cold exposures, once just before same planned cold exposures, and, if needed, right after the start of symptoms during same planned cold exposures
Other Name: Vascana
Placebo Comparator: Vehicle Drug: vehicle cream
0.5g of vehicle cream is topically administered BID for one day before certain planned cold exposures, once just before certain planned cold exposures, and, if needed, right after the start of symptoms during certain planned cold exposures

Detailed Description:

Raynaud's Phenomenon is a sometimes debilitating condition in which blood flow to the fingers or toes is compromised when a patient is exposed to cold or stress. Current therapies for Raynaud's are suboptimal because they are associated with significant side effects. In this study, patient responses to cold temperature exposures in a climate-controlled room after application of the study medication are measured.

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • clinical diagnosis of Raynaud's phenomenon as determined by a history of cold sensitivity with pain, numbness, and/or tingling along with pallor or cyanosis of the fingers
  • a history of at least two Raynaud's events during a typical winter day
  • must be willing to apply creams to fingers
  • must be willing to undergo cold temperature exposure
  • must be willing and able to stop certain medications
  • must be willing to use effective contraception, if applicable

Exclusion Criteria:

  • had a Raynaud's attack that required hospital or clinic intervention
  • has allergies to nitroglycerin or topical medication ingredients
  • has a history of migraine or chronic pain
  • has an unstable medical problem that could interfere with the study
  • had a heart attack or uncontrolled heart problems, hypertension, or hypotension in the past 3 months
  • used any investigational drug in the past 4 weeks
  • has significantly abnormal laboratory tests
  • had certain major surgeries in the past 6 months
  • has skin lesions on certain parts of the fingers
  • women who are pregnant or nursing
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00934427

Locations
United States, California
Stanford University
Redwood City, California, United States, 94063
United States, Connecticut
University of Connecticut
Farmington, Connecticut, United States, 06030
United States, Massachusetts
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
United States, Michigan
University of Michigan
Ann Arbor, Michigan, United States, 48106
Michigan State University
Grand Rapids, Michigan, United States, 49546
United States, Minnesota
University of Minnesota
Minneapolis, Minnesota, United States, 55455
United States, New Jersey
University of Medicine and Dentistry in New Jersey
New Brunswick, New Jersey, United States, 08903
United States, North Carolina
Carolina Arthritis
Wilmington, North Carolina, United States, 28401
United States, Ohio
Cleveland Clinic
Cleveland, Ohio, United States, 44195
University of Toledo
Toledo, Ohio, United States, 43614
United States, Wisconsin
Medical College of Wisconsin
Milwaukee, Wisconsin, United States, 53226
Sponsors and Collaborators
MediQuest Therapeutics
Investigators
Study Director: Jeff Gregory, MD MediQuest Therapeutics
  More Information

No publications provided

Responsible Party: Jeff Gregory, MD / Medical Director, MediQuest Therapeutics
ClinicalTrials.gov Identifier: NCT00934427     History of Changes
Other Study ID Numbers: 09-001
Study First Received: June 26, 2009
Last Updated: July 19, 2010
Health Authority: United States: Food and Drug Administration

Keywords provided by MediQuest Therapeutics:
Raynaud's
scleroderma
nitroglycerin
MQX-503
treatment

Additional relevant MeSH terms:
Raynaud Disease
Peripheral Vascular Diseases
Vascular Diseases
Cardiovascular Diseases
Nitroglycerin
Vasodilator Agents
Cardiovascular Agents
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on September 18, 2014